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Dive into the research topics where D. T. Bowen is active.

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Featured researches published by D. T. Bowen.


British Journal of Haematology | 1990

CUTANEOUS VASCULITIS IN PATIENTS WITH MYELODYSPLASIA

Anthony R. Green; D. Shuttleworth; D. T. Bowen; D. P. Bentley

We have recently encountered six patients with myelodyplasia (MDS) in whom biopsy proven cuteneous vasculitis was a major feature of their illness. In three patients there was, in addition, evidence of systemic vasculitis


Leukemia Research | 1990

Clonal growth of haemopoietic progenitor cells from myelodysplastic marrow in response to recombinant haemopoietins

Paul Baines; D. T. Bowen; A. Jacobs

The growth factor requirements of granulocyte-macrophage (GM) and erythroid marrow progenitor cells from 12 myelodysplastic (MDS) patients have been analysed. GM progenitors from two of six patients who grew normal numbers of colonies in response to conditioned medium + erythropoietin (5637CM + Epo) showed defective responses to either GMCSF and/or IL-3. Of all the recombinant factors tested (IL-3, IL-1, GCSF, GMCSF, MCSF), GMCSF was the strongest stimulator of myeloid clonal growth, inducing normal numbers of GM colonies from marrow of six patients (two of whom were neutropenic). Erythroid colonies were low in 5637CM + Epo-supplemented cultures of marrow from all but one patient and remained poor in the presence of any of the haemopoietins. tested. Supraoptimal doses (for normal marrow) of these haemopoietins improved colony growth in only one patient (GM colonies in response to IL-3). Combinations of factors were also largely ineffective at raising myeloid or erythroid colony numbers. These data indicate that the defective response of MDS progenitor cells to growth factors is not amenable to experimental manipulation of recombinant factor levels or combinations. Clonal assays might suggest a role for GMCSF therapy in a subpopulation of neutropenic MDS patients but their potential now needs to be evaluated in association with clinical trials.


Blood | 2000

Cytogenetic abnormalities in the myelodysplastic syndromes and occupational or environmental exposure

R. R. West; D. A. Stafford; A. D. White; D. T. Bowen; R. A. Padua


Leukemia | 1993

Two new polymorphisms but no mutations of the KIT gene in patients with myelodysplasia at positions corresponding to human FMS and murine W locus mutational hot spots

D. T. Bowen; R. A. Padua; Alan Kenneth Burnett; C. M. deCastro; R. E. Kaufman


Leukemia Research | 1995

Responsiveness to stem cell factor (SCF) of peripheral blood colony-forming cells from patients with myelodysplastic syndromes (MDS).

Gillian S. Masters; Paul Baines; Carol Tang; D. T. Bowen; Alan Kenneth Burnett


Blood | 2000

The presence of a FLT3 mutation in AML adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: Analysis of 854 patients from the MRC AML 10 and 12 trials

Pd Kottaridis; Rosemary E. Gale; Marion E. Frew; G Harrison; Stephen E. Langabeer; A. A. Belton; H. C. Walker; K. Wheatley; D. T. Bowen; Alan Kenneth Burnett; Ah Goldstone; David C. Linch


Archive | 2010

occupational or environmental exposure Cytogenetic abnormalities in the myelodysplastic syndromes and

Robert West; David A. Stafford; A. D. White; D. T. Bowen; Rose Ann Padua


Archive | 1997

Mutant RAS selectively promotes sensitivity of myeloid leukemia cells to apoptosis by a PKC-dependent process

Richard Lawrence Darley; A. Gallagher; D. T. Bowen; Alan Kenneth Burnett


Archive | 1993

In-vitro response of myeloid progenitors to phytohaemagglutin and interleukin-2 is related to survival of some myelodysplastic patients [Abstract]

G. B. Tennant; Ala I. Al-Sabah; Dominic Culligan; D. T. Bowen; A. Jacobs; Alan Kenneth Burnett


British Journal of Haematology | 1989

SECONDARY ERYTHROCYTOSIS AND SARCOIDOSIS

D. T. Bowen; Beatrix Wonke; P. M. Cotes

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Ah Goldstone

University College London

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David C. Linch

University College London

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G Harrison

Clinical Trial Service Unit

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H. C. Walker

Rutherford Appleton Laboratory

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K. Wheatley

Clinical Trial Service Unit

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